JCGGDB TOP Glycan Syntheses

Reaction

JCGG ID
JCGG-RAC0001589
Submitter
The Noguchi Institute
Reaction ID
R-0000-001589
Regist Date
2012/06/21 17:23:40
REACTANT
MOLECULE ID
JCGG-COM0002021 (Reaction Tree)
Reactant Type
donor
Mol
0.045 mmol
MOLECULE ID
JCGG-COM0000068 (Reaction Tree)
Skeleton
JCGG-STR032525
Reactant Type
acceptor
Mol
0.030 mmol
MOLECULE ID
JCGG-COM0000161
Reactant Type
promoter
Mol
0.027 mmol
PRODUCT
REACTION DETAIL
Reaction Time
120 hours
Reaction Temp
room temp
Solvent
ClCH2CH2Cl
Comment
The donor, the acceptor, and MS 4A were mixed and stirred for 1 hour before the reaction.
COMMENT
Keywords: carbohydrates, glycosides, glycosylation, oligosaccharides, synthetic methods
The reaction did not occur.
REFERENCE
Reference Id
REF-0000-000187
Issn
Electronic
Doi
10.1002/anie.201007212
PubMed ID
21433229
Journal Name
Angewandte Chemie (International ed. in English). (2011) 50 (18): 4197-201.
Article Title
S-Benzimidazolyl glycosides as a platform for oligosaccharide synthesis by an active-latent strategy.
Author
Scott J, Hasty; Matthew A, Kleine; Alexei V, Demchenko
Affiliation
Department of Chemistry and Biochemistry, University of Missouri-St.?Louis, One University Boulevard, St.?Louis, MO 63121, USA.
Reference Id
REF-0000-000188
Source
Angew. Chem. Int. Ed. 2011, 50, 4197-4201
Doi
10.1002/anie.201007212

©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)